View drug registration information details.
| Items | Registration information |
|---|
| ID | 809 |
|---|
| No | 809 |
|---|
| Brand Name | MAGNESIUM SULFATE 50 % |
|---|
| Ingredients | MAGNESIUM SULFATE 50 % |
|---|
| Dosage Form | INJECTION |
|---|
| Primary Packaging | AMPOULES |
|---|
| Storage | |
|---|
| Shelf Life | 3 YEARS |
|---|
| Pack Size | 10 ML/AMPOULE, 50 AMPOULES/BOX |
|---|
| Dispensing Category | |
|---|
| ATC Classification | |
|---|
| Pharmaceutical Class | |
|---|
| Indications | used to treat convulsions during pregnancy, nephritis in children, magnesium deficiency, and tetany |
|---|
| Contraindications | |
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| Side Effects | |
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| Unit Price | |
|---|
| EDL |
NULL |
|---|
| Description | CLEAR COLORLESS SOLUTION |
|---|
| Note | |
|---|
| License Owner | FACTORY NO. 3 |
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| Manufacturer | FACTORY NO. 3 |
|---|
| Country | LAO PDR |
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| Import Registration No | |
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| Import Registration Date | |
|---|
| Activity | CERTIFICATE RELEASED |
|---|
| Applied Date | |
|---|
| FDD Registration No | 01 L 1288/25 |
|---|
| FDD Registration Date | 03-FEB-2025 |
|---|
| Expiry Date | 02-FEB-2030 |
|---|
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